# FDA recall Z-0051-2020

> **Repro-Med Systems, Inc.** · Class II · device recall initiated 2019-08-20.

## Product

20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous  Safety Needle Sets"  Product # RMS22606 - Product Usage: RMS HlgH-Flo  Subcutaneous Safety Needle Sets are intended for the delivery of medication to the subcutaneous tissue.

## Reason for recall

Mislabeled needle lengths

## Distribution

US Nationwide distribution including the states of NJ, OH, FL, GA, IL, MA, CA, TX, NC, IA, NV, OR, MD, TN, VA, NY.

## Key facts

- **Recall number:** Z-0051-2020
- **Recalling firm:** Repro-Med Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-20
- **Report date:** 2019-10-16
- **Termination date:** 2020-05-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chester, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0051-2020

## Citation

> AI Analytics. FDA recall Z-0051-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0051-2020. Source: US FDA. Licensed CC0.

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